510(k) K023664 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
SYNTRA + DIALYZER, MODEL 200
| Applicant | Baxter Healthcare Corp, Mcgaw Park IL, US |
| Decision | Substantially Equivalent, Feb 21, 2003 |
| Received | Oct 31, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023664
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.